← Product Code [OLW](/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/OLW) · K003038

# AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A (K003038)

_Agilent Technologies Deutschland GmbH · OLW · Dec 15, 2000 · Neurology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/OLW/K003038

## Device Facts

- **Applicant:** Agilent Technologies Deutschland GmbH
- **Product Code:** [OLW](/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/OLW.md)
- **Decision Date:** Dec 15, 2000
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 882.1400
- **Device Class:** Class 2
- **Review Panel:** Neurology

## Regulatory Identification

An electroencephalograph is a device used to measure and record the electrical activity of the patient's brain obtained by placing two or more electrodes on the head.

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**Source:** [https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/OLW/K003038](https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/OLW/K003038)

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